Canonical Allele Identifier: CA814016462

Gene: ADCY2

Linked Data

• dbSNP Id: rs1180839562
• gnomAD v3: 5-7617089-T-C
• gnomAD v4: 5-7617089-T-C
• MyVariant Identifiers: chr5:g.7617202T>C (hg19) ; chr5:g.7617089T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7617089T>C , CM000667.2:g.7617089T>C	GRCh38
NC_000005.9:g.7617202T>C , CM000667.1:g.7617202T>C	GRCh37
NC_000005.8:g.7670202T>C	NCBI36
NG_046913.1:g.225860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.571-9078T>C MANE Select	ENSP00000342952.4:n.571-9078T>C
ENST00000338316.8:c.571-9078T>C	ENSP00000342952.4:n.571-9078T>C
ENST00000498598.1:n.270-9078T>C
ENST00000515681.1:c.-64+5914T>C	ENSP00000425069.1:n.-64+5914T>C
ENST00000537121.5:c.566-9078T>C	ENSP00000444803.2:n.566-9078T>C
NM_020546.2:c.571-9078T>C	NP_065433.2:n.571-9078T>C
XM_011513942.1:c.571-9078T>C	XP_011512244.1:n.571-9078T>C
XR_427657.2:n.585-9078T>C
XM_011513942.2:c.571-9078T>C	XP_011512244.1:n.571-9078T>C
XR_001741973.1:n.585-9078T>C
XR_001741974.2:n.585-9078T>C
NM_020546.3:c.571-9078T>C MANE Select	NP_065433.2:n.571-9078T>C